Medline recalls 32 PRE OP Kits containing B. Braun IV Administration Sets and Pump Administration Sets due to check valve components potentially getting stuck in open or closed positions.
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
Medline is recalling 32 different PRE OP Kits that contain B. Braun IV Administration Sets and Pump Administration Sets. The check valve components in these kits may become stuck in open or closed positions, which could lead to improper medication delivery.
The check valve components in these kits may become stuck in either open or closed positions. This could cause medication to not flow properly or be delivered at the wrong time, potentially leading to treatment errors.
Healthcare professionals and patients using these specific Medline PRE OP Kits for medical procedures. Those with the listed SKUs and lot numbers are most at risk.
Check for Medline PRE OP Kits with SKUs listed in the recall (e.g., DYKS1093B, DYKS1124C, etc.) and lot numbers starting with 25H through 25K.
Identify your Medline PRE OP Kit's SKU and lot number to see if it's in the recall list.
Reach out to Medline directly for assistance with the recall if you have the listed SKUs and lot numbers.
The recall is due to customer complaints that the check valve components in these kits may become stuck in open or closed positions.
Check for Medline PRE OP Kits with SKUs listed in the recall (e.g., DYKS1093B, DYKS1124C, etc.) and lot numbers starting with 25H through 25K.
Contact Medline directly for assistance with the recall if you have the listed SKUs and lot numbers.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1057-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1057-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
